Orphanet: SPG21

Search for a gene

* (*) mandatory field

SPG21 - SPG21 abhydrolase domain containing, maspardin

  • Synonym(s) : ABHD21, ACP33, BM-019, GL010, MAST
  • Previous symbols and names : SPG21, maspardin, spastic paraplegia 21 (autosomal recessive, Mast syndrome)
  • Type : gene with protein product
  • Chromosomal location : 15q22.31
  • OMIM: 608181
  • HGNC: 20373
  • UniProtKB: Q9NZD8
  • Genatlas: SPG21
  • Ensembl: ENSG00000090487
  • IUPHAR-DB: -
  • Reactome: Q9NZD8
  • LOVD: SPG21

Diseases list

  : Assessed

Gene included in a panel of genes performed as part of a diagnostic test

Additional information

Health care resources for this gene

Specialised Social Services

The documents contained in this web site are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.

Orphanet is part of the Gene Curation Coalition, a global effort to harmonise gene-level resources.